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CLC Genomics Workbench
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QIAGEN CLC Genomics Workbench is a powerful solution that works for everyone, no matter the workflow. Cutting-edge technology, unique featur...
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SARS-CoV-2 Solutions
Introducing QCI Interpret Translational
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Discover a new software solution for NGS variant annotation, filtering, and triage of human exome sequencing data.
Human Gene Mutations Database (HGMD)
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Solve more cases faster, with data you can trust using HGMD Professional, the gold standard for identifying inherited disease-causing mutati...
Accurate and efficient interpretation with QCI Precision Insights, now available in Europe
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As next-generation DNA sequencing technology continues to evolve and become further integrated into routine clinical testing, the need for e...
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Build on the knowledge of millions to unlock new scientific discoveries. With over 20 million findings and more than 500,000 datasets, our p...
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Clinical and Economic Value of Genetic Sequencing for Personalized Therapy
QIAGEN CLC training – 2 part series Jan 26-27
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Join us for a two-day 60 minute training series on QIAGEN CLC Version 21. During these two days, we will introduce you to key features of QI...
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Dig into the details and get inspired!
Application notes
“External Applications”: adding functionalities to the CLC Genomics Server
A Sample to Insight® NGS solution for myeloid neoplasms: Redefined amplicon sequencing for low variant detection and interpretation
CLC Server Command Line Tools: a powerful choice to optimize your analyses
Comparative Analysis of Endophytic Bacterial Microbiomes in Grapevine
Comparative analysis of three bovine genomes
Example queries for HGMD MySQL Database
Improving Microbiome Sequencing using QIAseq® 16S/ITS Panels
Improving structural annotation in complex genomes with QIAGEN CLC Genomics Workbench
QIAseq Targeted Panel Analysis
Whole Exome Sequencing Benchmark
Whole genome functional annotation of Solanum lycopersicum
White papers
A comprehensive analysis of coregulator recruitment, androgen receptor function and gene expression in prostate cancer
Analyzing whole human genomes for as little as $22
Challenges in Clinical Testing
Characterizing the Microbiome through Targeted Sequencing of Bacterial 16S rRNA and Fungal ITS Regions
Chip-seq Analysis
CLC read mapper
Copy number variant detection
De novo assembly
Discovering the functional potential of microbial communities through whole metagenome shotgun sequencing analysis
Dynamics in the airway microbiome in children with Cystic fibrosis as revealed by 16S rRNA gene sequencing
Phenotype-Driven Ranking filter
Probabilistic Variant Caller 1.1
TET2 binds the androgen receptor and loss is associated with prostate cancer
Transcription factor ChIP-seq
Understanding Breast Cancer Subtypes by Jointly Interpreting Tumor Genomes and Transcriptomes